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  1. No Access

    Article

    Determination of Physiological Indices and Some Antioxidant Enzymes of Chard Exposed to Nitric Oxide under Drought Stress

    This research was carried out to determine effectiveness of nitric oxide (NO) on some physiological and biochemical reactions, and water use efficiency (WUE) of chard (Beta vulgaris L. var. cicla) under well-wate...

    M. Ekinci, S. Ors, E. Yildirim, M. Turan, U. Sahin… in Russian Journal of Plant Physiology (2020)

  2. No Access

    Article

    The IL-1RN and IL-4 gene polymorphisms are potential genetic markers of susceptibility to bladder cancer: a case–control study

    We investigated the relationship between the distribution of the IL-1RN, TNF-β and IL-4 polymorphism and the clinical features of bladder cancer.

    S. T. Bozdoğan, B. Erol, A. Dursun, G. Bozdoğan, I. Dönmez… in World Journal of Urology (2015)

  3. No Access

    Article

    Spectrum of Brevundimonas vesicularis infections in neonatal period: a case series at a tertiary referral center

    To report infections caused by Brevundimonas vesicularis and the treatment regimens administered based on antibiotic studies of this Gram-negative bacterium in the neonatal period.

    N. Karadag, B. S. Karagol, A. A. Kundak, A. Dursun, N. Okumus, G. Tanır… in Infection (2012)

  4. No Access

    Chapter

    Identification of Mutations and Evaluation of Cardiomyopathy in Turkish Patients with Primary Carnitine Deficiency

    Primary systemic carnitine deficiency (SCD) is an autosomal recessive disorder caused by defective cellular carnitine transport. Patients usually present with predominant metabolic or cardiac manifestations. S...

    M. Kilic, R. K. Özgül, T. Coşkun, D. Yücel… in JIMD Reports - Case and Research Reports, … (2012)

  5. No Access

    Chapter

    A Zinc Sulphate-Resistant Acrodermatitis Enteropathica Patient with a Novel Mutation in SLC39A4 Gene

    Acrodermatitis enteropathica (AE) is a rare autosomal recessive disorder of zinc deficiency due to an abnormal intestinal zinc transporter. It is characterized by the triad of acral dermatitis, alopecia, and d...

    M. Kilic, M. Taskesen, T. Coskun, F. Gürakan… in JIMD Reports - Case and Research Reports, … (2012)

  6. No Access

    Chapter

    Mutation Spectrum of Fumarylacetoacetase Gene and Clinical Aspects of Tyrosinemia Type I Disease

    Tyrosinemia type I (OMIM 276700) is a rare, autosomal recessive disorder caused by a deficiency in the fumarylacetoacetate hydrolase (FAH) enzyme. This study examined the spectrum of FAH gene mutation in 32 patie...

    A. Dursun, R. K. Özgül, S. Sivri, A. Tokatlı… in JIMD Reports - Case and Research Reports, … (2011)

  7. Article

    1279 A Nested Case-Control Study for Risk Factors of Infantile Colic

    Backgroud and aims: To analyse infantile (birth characteristics, feeding type) and environmental (maternal smoking, nutrition and psychological status, mother-child bonding, family structure, support to mother...

    S S Yalcin, E Orun, B Mutlu, Y Madendag, I Sinici, A Dursun… in Pediatric Research (2010)

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  8. No Access

    Article

    Four novel PDHA1 mutations in pyruvate dehydrogenase deficiency

    The pyruvate dehydrogenase (PDH) complex is a mitochondrial multienzyme that catalyses the irreversible oxidative decarboxylation of pyruvate to acetyl-CoA. We report four novel PDHA1 mutations in patients with p...

    E. Ostergaard, L. Birk Moller… in Journal of Inherited Metabolic Disease (2009)

  9. No Access

    Article

    Does maternal knowledge impact blood phenylalanine concentration in Turkish children with phenylketonuria?

    The aim of this study was to compare the level of maternal knowledge and the blood phenylalanine (Phe) control in phenylketonuria (PKU; OMIM 261600). The study was conducted on 144 children (81 boys, 63 girls)...

    H. Gokmen Ozel, T. Kucukkasap, G. Koksal… in Journal of Inherited Metabolic Disease (2008)

  10. No Access

    Article

    Neurocutaneous melanosis associated with Dandy-Walker malformation

    Neurocutaneous melanosis is an uncommon congenital disorder consisting of benign or malignant melanocytic tumors of the leptomeninges with large or numerous cutaneous congenital melanocytic nevi. The Dandy-Wal...

    M. Kalaycı, F. Çağavi, U. Bayar, Ş. Gül, A. Dursun, B. Ermis… in Acta Neurochirurgica (2006)

  11. No Access

    Article

    Detection ofCandida albicans by culture, serology and PCR in clinical specimens from patients with ulcerative colitis: Re-evaluation of an old hypothesis with a new perspective

    The relationship between inflammatory bowel disease and microorganisms was evaluated. The presence ofCandida albicans-specific IgM and IgG antibodies in serum samples and the presence ofC. albicans in stool and c...

    A. Kalkanci, C. Tuncer, B. Degertekin, A. Eren, S. Kustimur… in Folia Microbiologica (2005)

  12. No Access

    Article

    Formation of nanoporous platinum by selective dissolution of Cu from Cu0.75Pt0.25

    This paper gives results demonstrating the production of nanoporous platinum through the de-alloying of Cu0.75Pt0.25 alloy in 1 M H2SO4. Both field emission scanning electron microscopy and small angle neutron sc...

    D. V. Pugh, A. Dursun, S. G. Corcoran in Journal of Materials Research (2003)

  13. No Access

    Article

    Maple syrup urine disease: Mutation analysis in Turkish patients

    Maple syrup urine disease (MSUD), the most frequently occurring organic acidaemia in Turkey, is caused by a deficiency of the activity of branched-chain keto acid dehydrogenase enzyme (BCKAD) complex. Mutation...

    A. Dursun, M. Henneke, K. Özgül, J. Gartner… in Journal of Inherited Metabolic Disease (2002)

  14. No Access

    Article

    Mutation analysis in Turkish patients with hereditary fructose intolerance

    Thirteen Turkish patients with hereditary fructose intolerance (HFI) were screened for the three common mutations, A149P, A174D and N334K, in the aldolase B gene that have been detected frequently in European ...

    A. Dursun, H. S. Kalkanoğlu, T. Coşkun… in Journal of Inherited Metabolic Disease (2001)

  15. No Access

    Article

    Neuroleptic malignant syndrome in a patient with citrullinaemia

    A. Dursun, Y. Yilmaz, M. Özsari, N. Kandemir… in Journal of Inherited Metabolic Disease (2000)

  16. No Access

    Chapter

    Effect of micro-element application on mineral composition and yield of spinach (spinacia oleracea) grown in soils with different lime contents

    This study was undertaken to determine the effects of soil or foliage applied microplex fertilizer (5.4 %Mg, 4% Mn, 4% Fe, 1.5 % Cu, 1.5 % Zn, 0.5 % B, 0.1 % Mo and 0.05 % Co) on dry matter and mineral content...

    A. Aydin, M. Turan, A. Dursun in Improved Crop Quality by Nutrient Management (1999)

  17. No Access

    Chapter

    Macro and micro nutrient contents of tomato (Lycopersicon esculentum) and eggplant (Solatium melongena var. Esculentum) seedlings and their effects on seedling growth in relation to humic acid application

    Plant performance mainly depends on characteristics of photosynthetically active organs. Many of these characteristics such as growth performance and quality of seedlings are modified by ecological conditions ...

    A. Dursun, İ Güver, M. Turan in Improved Crop Quality by Nutrient Management (1999)

  18. No Access

    Article

    Incisional healing in rats treated with diethyl maleate

    Diethyl maleate (DEM) which binds and thus depletes tissue glutathione levels was used to aggravate the injury and to determine its effect on incisional healing. A 5 cm dorsal midline skin incision was perform...

    R. Yavuzer, Ö. Tascilar, E. Tekin, O. Latifoğlu… in European Journal of Plastic Surgery (1997)

  19. No Access

    Article

    Neutral lipid storage disease co-existing with ichthyosiform dermatosis

    A. Dursun, A. Kubar, A. Gokoz, F. Duru, A. Gürgey in European Journal of Pediatrics (1994)